EP0612804A2 - Ölabweisende Fluorkautschukzusammensetzung - Google Patents

Ölabweisende Fluorkautschukzusammensetzung Download PDF

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Publication number
EP0612804A2
EP0612804A2 EP94301230A EP94301230A EP0612804A2 EP 0612804 A2 EP0612804 A2 EP 0612804A2 EP 94301230 A EP94301230 A EP 94301230A EP 94301230 A EP94301230 A EP 94301230A EP 0612804 A2 EP0612804 A2 EP 0612804A2
Authority
EP
European Patent Office
Prior art keywords
fluororubber
oil
composition
molecular weight
repellent
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
EP94301230A
Other languages
English (en)
French (fr)
Other versions
EP0612804B1 (de
EP0612804A3 (en
Inventor
Noritomo C/O Kinyosha Co. Ltd. Fukunaga
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Kinyosha Co Ltd
Original Assignee
Kinyosha Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Kinyosha Co Ltd filed Critical Kinyosha Co Ltd
Publication of EP0612804A2 publication Critical patent/EP0612804A2/de
Publication of EP0612804A3 publication Critical patent/EP0612804A3/en
Application granted granted Critical
Publication of EP0612804B1 publication Critical patent/EP0612804B1/de
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Classifications

    • G—PHYSICS
    • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
    • G03G15/00—Apparatus for electrographic processes using a charge pattern
    • G03G15/20—Apparatus for electrographic processes using a charge pattern for fixing, e.g. by using heat
    • G03G15/2003—Apparatus for electrographic processes using a charge pattern for fixing, e.g. by using heat using heat
    • G03G15/2014—Apparatus for electrographic processes using a charge pattern for fixing, e.g. by using heat using heat using contact heat
    • G03G15/2053—Structural details of heat elements, e.g. structure of roller or belt, eddy current, induction heating
    • G03G15/2057—Structural details of heat elements, e.g. structure of roller or belt, eddy current, induction heating relating to the chemical composition of the heat element and layers thereof
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00—Use of inorganic substances as compounding ingredients
    • C08K3/01—Use of inorganic substances as compounding ingredients characterized by their specific function
    • C08K3/013—Fillers, pigments or reinforcing additives
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00—Use of inorganic substances as compounding ingredients
    • C08K3/02—Elements
    • C08K3/08—Metals
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L27/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers
    • C08L27/02—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C08L27/12—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment containing fluorine atoms
    • C08L27/18—Homopolymers or copolymers or tetrafluoroethene
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L27/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers
    • C08L27/22—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers modified by chemical after-treatment
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2205/00—Polymer mixtures characterised by other features
    • C08L2205/02—Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00—Stock material or miscellaneous articles
    • Y10T428/13—Hollow or container type article [e.g., tube, vase, etc.]
    • Y10T428/1352—Polymer or resin containing [i.e., natural or synthetic]
    • Y10T428/1372—Randomly noninterengaged or randomly contacting fibers, filaments, particles, or flakes

Definitions

  • the present invention relates to an oil-repellent fluororubber composition, and, more specifically, to an oil-repellent fluororubber composition prepared by compounding a low-molecular weight ethylene tetrafluoride resin to a peroxide crosslinked fluororubber having a Mooney viscosity of 90 or more ML1+10 (100 °C) or compounding a low-molecular weight ethylene tetrafluoride resin and an inorganic filler selected from the powders of solid substances having surface energy higher than that of copper to a peroxide crosslinked fluororubber.
  • fluororubber products have been used primarily as heat-resistant and oil-resistant materials for oil seal components for cars, diaphragms, tubes, hoses, gaskets and O-rings, as packing materials for chemical resistance, as sealing materials for ozone resistance and as wire coating materials, their excellent heat resistance, oil resistance, chemical resistance, solvent resistance and high-corrosive gas resistance being utilized.
  • fluororubber products hardly have oil repellency as is described hereunder and hence are poor in oil resistance to some kinds of oils, not showing sufficient endurance.
  • some attempts to impart oil repellency to fluororubber products have been taken with a view to improving endurance, and various methods have been proposed. The methods are divided largely into 1) methods of modifying the surface of a fluororubber product and 2) methods of modifying the composition of a fluororubber composition.
  • a treatment according to fluorine gas a treatment according to chemicals having reactivity with fluororubbers and, as a more general method, surface coating with a fluorine resin (selected from a polytetrafluoroethylene resin, an ethylene tetrafluoride-perfluorovinyl ether copolymer resin, an ethylene tetrafluoride-propylene hexafluoride copolymer resin and the like according to temperature conditions for use).
  • a fluorine resin selected from a polytetrafluoroethylene resin, an ethylene tetrafluoride-perfluorovinyl ether copolymer resin, an ethylene tetrafluoride-propylene hexafluoride copolymer resin and the like according to temperature conditions for use.
  • fluororubber products subjected to a surface treatment come to lose oil repellency due to the breakage and peeling of the surface layer caused by repeated loading in use (compression, abrasion, extension, etc.).
  • products from the composition with only a fluorine resin powder compounded therein do not lose oil-repellency in use, but they deteriorate in their rubber strength and physical properties, particularly, in their extension; hence both cannot be said to be satisfactory modifications.
  • the object of the present invention is to provide an oil-repellent fluororubber elastomer having excellent oil repellency hardly impaired in use and in addition having sufficient mechanical and physical characteristics which a fluororubber elastomer originally possesses.
  • an oil-repellent fluororubber composition prepared by compounding a low-molecular weight ethylene tetrafluoride resin to a peroxide crosslinked fluororubber having a Mooney viscosity of 90 or more ML1+10 (100 °C) (a first invention) or compounding a low-molecular weight ethylene tetrafluoride resin and an inorganic filler selected from the powders of solid substances having surface energy higher than that of copper to a peroxide crosslinked fluororubber (a second invention) can be obtained.
  • crosslinking methods of a fluororubber such methods taking advantage of the characteristics of polymers as amine crosslinking, polyol crosslinking, peroxide crosslinking and the like, and in addition, the development of polymers suitable for each crosslinking method has been conducted.
  • the peroxide-type fluorororubber to be used in the present invention is a flurorubber having halogen, particularly, bromine and/or iodine and a hydrogen atom introduced into the terminal of a polymer molecular chain and the side chain, and crosslinking is conducted according to a drawing reaction of a halogen atom and a hydrogen atom.
  • crosslinking is carried out in a conventional manner, using a radical generator represented by an organic peroxide compound as a crosslinking agent and a crosslinking auxiliary, generally triallyl isocyanurate.
  • peroxide crosslinked fluororubber those having a high molecular weight with a Mooney viscosity of 90 or more ML1+10 (100 °C) are preferable. As is shown in Comparative Test to be described later, those with a low Mooney viscosity cannot form an elastomer having sufficient oil repellency.
  • a low-molecular weight ethylene tetrafluoride resin to be used as an oil-repellency imparting agent in the present invention is a polymer of ethylene tetrafluoride having a molecular weight of the order of 103 to 105, and it has been used as an additive for the decrease of the coefficient of dynamic friction, the improvement of abrasion resistance or the improvement of tear strength of rubber, plastics, oil, ink and paints.
  • Commercially available examples include Lubron* L-5, L-2 (Daikin Kogyo), MP * 1100, 1200, 1300, 1400, 1500, and TLP * -10F-1 (Mitsui-DuPont Fluorochemicals) (*: trademark, hereunder same as above).
  • the compounding ratio of a low-molecular weight ethylene tetrafluoride resin is not particularly restricted, it is preferable to compound 60 weight parts or more of it based on 100 weight parts of a fluororubber in order to impart sufficient oil repellency.
  • An ethylene tetrafluoride resin to, be used for forming has a high molecular weight of the order of 106, and it is difficult to compound such a resin in a fluororubber in a large amount and uniformly and, therefore, it is not suited to be used in the present invention.
  • a second invention is characterized by the point that an inorganic filler comprising a solid element and/or an inorganic compound powder having surface energy higher than that of copper is compounded in an oil-repellent fluororubber composition in addition to a low-molecular weight ethylene tetrafluoride resin.
  • MT carbon black, or an inorganic filler such as powders of silica, alumina and copper is compounded in order to improve the rubber strength and physical properties of fluororubber.
  • the present inventor made studies about the properties, functions and effects of various inorganic fillers. As a result, he has found that, contrary to the general anticipation regarding the wetting of a solid material and surface energy, by the use of an inorganic material having extremely high surface energy, particularly a powder of a solid material (a solid element and a solid inorganic compound) having surface energy higher than that of copper, the effects according to a first invention, that is, the strength and physical properties, can be imparted without impairing excellent oil repellency. This finding has led to the completion of a second invention. Specific examples of inorganic fillers preferably used in Examples of a second invention are powders of iron, nickel, cobalt, iron-cobalt alloy, molybdenum, tungsten, tantalum and tungsten-carbide.
  • the compounding amount of these inorganic fillers is not particularly restricted; from the viewpoints of the rubber strength and physical properties, however, it is preferably used in an amount of 20 weight parts or more based on 100 weight parts of a fluororubber.
  • a powder preferably used as an inorganic filler has an average particle diameter of 1-15 ⁇ m or less. Powders with an average particle diameter of more than 15 ⁇ m separate from vulcanized rubber products and may impair their smoothness.
  • a sheet of 10 mm x 30 mm x 1 mm thickness was prepared from each rubber. One side of a sheet was abraded with a sandpaper #1200 to prepare a test sample.
  • the test sample was provided in a surface tension measuring instrument manufactured by Kyowa Kagaku, and dimethyl polysiloxane oil with a viscosity of 50 cSt. was dropped on the test sample at room temperature (25 °C) to measure the contact angle ( ⁇ °), a criterion of oil repellency.
  • the ⁇ ° of an ordinary fluororubber elastomer measured according to this test was 0°, which showed that it was substantially non-oil-repellent.
  • a particle of an inorganic filler to be used in the present invention is not restricted to a particle of a single material. It may have a double constitution of a core of a material with low surface energy and a coating layer of a material with high surface energy.
  • Vulcanizing conditions can also be changed properly. Though standard oven heating conditions are 180 °C and 4 hours, they may be 250 °C and 24 hours. Besides, primary vulcanization and secondary oven heating can be conducted in vacuum or in inactive gas such as carbon dioxide gas, helium gas, argon gas or nitrogen gas. In primary vulcanization and/or secondary heating, radiations can also be utilized. If desired, ultraviolet-light irradiation or a fluorine gas treatment can be employed in a crosslinked rubber.
  • inactive gas such as carbon dioxide gas, helium gas, argon gas or nitrogen gas.
  • radiations can also be utilized. If desired, ultraviolet-light irradiation or a fluorine gas treatment can be employed in a crosslinked rubber.
  • the following substances can be compounded in the oil-repellent fluororubber composition of the present invention in such a range as would not substantially impair its excellent oil repellency in order to impart or improve special properties.
  • Improvement of the physical characteristics of rubbers carbon black such as MT and FT
  • Imparting of conductivity Ketchen black (Ketchen* EC), acetylene black, carbon fiber, conductive metal coating powder, inorganic and ceramic whisker powder
  • Prevention of static electrification various antistatic agents, surfactants Improvement of abrasion resistance: mica powder and the like
  • Imparting of processability thermoplastic fluororubber (Daiel* thermoplastics), low-molecular weight liquid flurororubber (Daiel* G-101) and fluorosilicone oil and fluorosilicone rubber, fluorine oil Compatibility improving agents and thermoresistance additives: silicone oil and reactive silicone oil, silicone resin, silicone coupling agents
  • Low-temperature properties imparting agent vinyl silicone rubber
  • a compound was prepared from 4 kinds of peroxide crosslinked fluororubbers with different Mooney viscosities according to the following compounding recipe.
  • Compounding weight parts
  • Example 4 Influence of the compounding amount of low-molecular weight ethylene tetrafluoride
  • Example 5 Influence of the kinds and the compounding amount of inorganic fillers
  • Example 3 The same procedure as in Example 3 was repeated except that the kinds and the compounding amount of inorganic fillers were changed.
  • An oil-repellent fluororubber elastomer having excellent oil repellency and at the same time maintaining original mechanical and physical characteristics sufficiently can be obtained, using easily available materials on the market without any special means of processing and treatment.

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  • Chemical & Material Sciences (AREA)
  • Polymers & Plastics (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Organic Chemistry (AREA)
  • General Physics & Mathematics (AREA)
  • Physics & Mathematics (AREA)
  • General Chemical & Material Sciences (AREA)
  • Fixing For Electrophotography (AREA)
  • Rolls And Other Rotary Bodies (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Laminated Bodies (AREA)
EP94301230A 1993-02-22 1994-02-22 Ölabweisende Fluorkautschukzusammensetzung Expired - Lifetime EP0612804B1 (de)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP5465393 1993-02-22
JP54653/93 1993-02-22
JP5054653A JP2876375B2 (ja) 1993-02-22 1993-02-22 ロール

Publications (3)

Publication Number Publication Date
EP0612804A2 true EP0612804A2 (de) 1994-08-31
EP0612804A3 EP0612804A3 (en) 1995-11-02
EP0612804B1 EP0612804B1 (de) 2000-08-23

Family

ID=12976749

Family Applications (2)

Application Number Title Priority Date Filing Date
EP94301231A Expired - Lifetime EP0613068B1 (de) 1993-02-22 1994-02-22 Rolle
EP94301230A Expired - Lifetime EP0612804B1 (de) 1993-02-22 1994-02-22 Ölabweisende Fluorkautschukzusammensetzung

Family Applications Before (1)

Application Number Title Priority Date Filing Date
EP94301231A Expired - Lifetime EP0613068B1 (de) 1993-02-22 1994-02-22 Rolle

Country Status (5)

Country Link
US (2) US5399142A (de)
EP (2) EP0613068B1 (de)
JP (1) JP2876375B2 (de)
CA (2) CA2115970C (de)
DE (2) DE69425597T2 (de)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0683438A2 (de) * 1994-05-18 1995-11-22 Bridgestone Corporation Papierzuführwalze sowie -gerät
EP0829514A2 (de) * 1996-09-13 1998-03-18 Pall Corporation Oleophobe-hydrophobe Fluorpolymerzusammensetzungen
EP1935939A1 (de) * 2005-10-12 2008-06-25 NOK Corporation Ptfe-harzzusammensetzung

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP3514155B2 (ja) * 1999-02-19 2004-03-31 富士写真光機株式会社 内視鏡装置
JP3733862B2 (ja) * 2001-02-01 2006-01-11 東海ゴム工業株式会社 燃料輸送用ホース装置
JP3966464B2 (ja) * 2002-04-03 2007-08-29 日産自動車株式会社 シールリング及びシール装置
JP3966474B2 (ja) * 2003-10-02 2007-08-29 日産自動車株式会社 シールリング及びシール装置
US7854819B2 (en) * 2005-05-17 2010-12-21 Panasonic Corporation Multilayer information recording medium and production method therefor
JP5821348B2 (ja) * 2011-07-08 2015-11-24 ダイキン工業株式会社 定着用ロール及び定着用ベルト
JP6425371B2 (ja) * 2012-08-02 2018-11-21 キヤノン株式会社 定着部材及びその製造方法、定着装置、画像形成装置
US9251927B2 (en) * 2012-08-13 2016-02-02 Joinset Co., Ltd. Cable having reduced tangle ability
CN105722680B (zh) * 2013-11-15 2020-08-25 大金工业株式会社 层积体、层积体的制造方法和氟橡胶组合物
WO2015118810A1 (ja) 2014-02-05 2015-08-13 キヤノン株式会社 定着部材とその製造方法、定着装置および画像形成装置
US20200299533A1 (en) * 2017-12-18 2020-09-24 3M Innovative Properties Company Fluorinated elastomers cured by actinic radiation and methods thereof

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Publication number Priority date Publication date Assignee Title
FR2288763A1 (fr) * 1974-10-21 1976-05-21 Allied Chem Compositions comprenant des melanges de copolymeres 3,3,3-trifluoro-2-trifluoromethylpropene/fluorure de vinylidene et de poly-tetrafluoroethylene
EP0310966A1 (de) * 1987-10-02 1989-04-12 AUSIMONT S.p.A. Additive zum Erleichtern des Abtrennens der Gussformen von mit Peroxiden vulkanisierbarem Kautschuk

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EP0310966A1 (de) * 1987-10-02 1989-04-12 AUSIMONT S.p.A. Additive zum Erleichtern des Abtrennens der Gussformen von mit Peroxiden vulkanisierbarem Kautschuk

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PREPRINTS OF THE 138TH MEETING FALL '90, PAPER 75, WASHINGTON US R.A.MORGAN ET AL 'reinforcement of elastomers with fluoroplastic additives' *

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0683438A2 (de) * 1994-05-18 1995-11-22 Bridgestone Corporation Papierzuführwalze sowie -gerät
EP0683438A3 (de) * 1994-05-18 1996-03-13 Bridgestone Corp Papierzuführwalze sowie -gerät.
US5723214A (en) * 1994-05-18 1998-03-03 Bridgestone Corporation Paper feed roll and apparatus
EP0829514A2 (de) * 1996-09-13 1998-03-18 Pall Corporation Oleophobe-hydrophobe Fluorpolymerzusammensetzungen
EP0829514A3 (de) * 1996-09-13 1998-04-22 Pall Corporation Oleophobe-hydrophobe Fluorpolymerzusammensetzungen
US5981614A (en) * 1996-09-13 1999-11-09 Adiletta; Joseph G. Hydrophobic-oleophobic fluoropolymer compositions
EP1935939A1 (de) * 2005-10-12 2008-06-25 NOK Corporation Ptfe-harzzusammensetzung
EP1935939A4 (de) * 2005-10-12 2011-03-23 Nok Corp Ptfe-harzzusammensetzung

Also Published As

Publication number Publication date
DE69425597D1 (de) 2000-09-28
CA2115970A1 (en) 1994-08-23
DE69433891T2 (de) 2005-08-04
JPH06250553A (ja) 1994-09-09
EP0612804B1 (de) 2000-08-23
CA2115970C (en) 2000-11-28
EP0612804A3 (en) 1995-11-02
US5399142A (en) 1995-03-21
CA2115962A1 (en) 1994-08-23
US5428096A (en) 1995-06-27
CA2115962C (en) 2000-07-25
JP2876375B2 (ja) 1999-03-31
DE69425597T2 (de) 2001-05-23
EP0613068A3 (de) 1995-09-20
EP0613068A2 (de) 1994-08-31
EP0613068B1 (de) 2004-07-14
DE69433891D1 (de) 2004-08-19

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